IL153594A0 - Amino alcohol derivatives and pharmaceutical compositions containing the same - Google Patents

Amino alcohol derivatives and pharmaceutical compositions containing the same

Info

Publication number
IL153594A0
IL153594A0 IL15359401A IL15359401A IL153594A0 IL 153594 A0 IL153594 A0 IL 153594A0 IL 15359401 A IL15359401 A IL 15359401A IL 15359401 A IL15359401 A IL 15359401A IL 153594 A0 IL153594 A0 IL 153594A0
Authority
IL
Israel
Prior art keywords
group
hydrogen atom
same
pharmaceutical compositions
compositions containing
Prior art date
Application number
IL15359401A
Original Assignee
Sankyo Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sankyo Co filed Critical Sankyo Co
Publication of IL153594A0 publication Critical patent/IL153594A0/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/001—Amines; Imines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/16—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/32—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/002—Nitriles (-CN)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/008—Preparation of nitrogen-containing organic compounds containing a N-O bond, e.g. nitro (-NO2), nitroso (-NO)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The present invention relates to compounds of formula (I) which exhibit excellent immune suppression activity, pharmacologically acceptable salts thereof, esters thereof or other derivatives: <CHEM> wherein R<1> and R<2> are a hydrogen atom, an amino protecting group; R<3> is a hydrogen atom, a hydroxy protecting group; R<4> is a lower alkyl group; n is an integer from 1 to 6; X is an ethylene group; Y is a C1-C10 alkylene group, a C1-C10 alkylene group substituted with 1 to 3 substituents selected from substituent group a and b; R<5> is an aryl group; R<6> and R<7> are a hydrogen atom, a group selected from substituent group a; with the proviso when R<5> is a hydrogen atom, Y is not a single bond or a straight chain C1-C10 alkylene group.
IL15359401A 2000-07-13 2001-07-10 Amino alcohol derivatives and pharmaceutical compositions containing the same IL153594A0 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2000212246 2000-07-13
JP2000241744 2000-08-09
JP2000283218 2000-09-19
PCT/JP2001/005988 WO2002006268A1 (en) 2000-07-13 2001-07-10 Amino alcohol derivatives

Publications (1)

Publication Number Publication Date
IL153594A0 true IL153594A0 (en) 2003-07-06

Family

ID=27344040

Family Applications (3)

Application Number Title Priority Date Filing Date
IL15359401A IL153594A0 (en) 2000-07-13 2001-07-10 Amino alcohol derivatives and pharmaceutical compositions containing the same
IL153594A IL153594A (en) 2000-07-13 2002-12-22 Amino alcohol derivatives and pharmaceutical compositions containing the same
IL174664A IL174664A0 (en) 2000-07-13 2006-03-30 Optically active amino alcohol derivatives and processes for the preparation thereof

Family Applications After (2)

Application Number Title Priority Date Filing Date
IL153594A IL153594A (en) 2000-07-13 2002-12-22 Amino alcohol derivatives and pharmaceutical compositions containing the same
IL174664A IL174664A0 (en) 2000-07-13 2006-03-30 Optically active amino alcohol derivatives and processes for the preparation thereof

Country Status (20)

Country Link
US (2) US6723745B2 (en)
EP (1) EP1300405B1 (en)
KR (1) KR100812578B1 (en)
CN (2) CN1328387C (en)
AT (1) ATE360011T1 (en)
AU (2) AU2001269503B2 (en)
BR (1) BR0112484A (en)
CA (1) CA2415678A1 (en)
CZ (1) CZ200350A3 (en)
DE (1) DE60127961D1 (en)
HK (1) HK1051680A1 (en)
HU (1) HUP0301688A3 (en)
IL (3) IL153594A0 (en)
MX (1) MXPA03000397A (en)
NO (1) NO20030120L (en)
NZ (2) NZ533997A (en)
PL (1) PL359411A1 (en)
SK (1) SK152003A3 (en)
TW (1) TWI301833B (en)
WO (1) WO2002006268A1 (en)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8882847B2 (en) 2001-05-25 2014-11-11 Conformis, Inc. Patient selectable knee joint arthroplasty devices
CZ200350A3 (en) * 2000-07-13 2003-05-14 Sankyo Company Limited Aminoalcohol derivatives
WO2002029001A2 (en) 2000-10-03 2002-04-11 University Of Virginian Patent Foundation Novel lysophosphatidic acid receptor agonists and antagonists
WO2002064616A2 (en) 2001-01-30 2002-08-22 University Of Virgina Patent Foundation Agonists and antagonists of sphingosine-1-phosphate receptors
ATE314383T1 (en) * 2001-03-26 2006-01-15 Novartis Pharma Gmbh 2-AMINO-PROPANOL DERIVATIVES
DE60328161D1 (en) * 2002-01-11 2009-08-13 Daiichi Sankyo Co Ltd AMINO ALCOHOL DERIVATIVE OR PHOSPHONIC ACID DERIVATIVE AND MEDICAL COMPOSITION CONTAINING THEREOF
EP1478641A1 (en) * 2002-01-24 2004-11-24 Eli Lilly And Company Process for preparing an intermediate useful for the asymmetric synthesis of duloxetine
SI1505959T1 (en) 2002-05-16 2009-04-30 Novartis Ag Use of edg receptor binding agents in cancer
SE0202280D0 (en) * 2002-07-19 2002-07-19 Astrazeneca Ab Novel compounds
SE0202279D0 (en) * 2002-07-19 2002-07-19 Astrazeneca Ab Novel comppounds
EP1548003A4 (en) 2002-09-19 2006-06-07 Kyorin Seiyaku Kk Amino alcohol derivative, addition salt thereof, and immunosuppressant
KR20080103117A (en) 2002-09-24 2008-11-26 노파르티스 아게 Sphingosine-1-phosphate receptor agonists in the treatment of demyelinating disorders
US7452911B2 (en) 2002-10-31 2008-11-18 Boehringer Ingelheim Pharma Gmbh & Co. Kg Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
EP3075356B1 (en) 2002-11-07 2023-07-05 ConforMIS, Inc. Method of selecting a meniscal implant
CA2707750A1 (en) 2003-04-08 2004-10-21 Novartis Ag Solid pharmaceutical compositions comprising a s1p receptor agonist and a sugar alcohol
WO2005005383A1 (en) * 2003-07-11 2005-01-20 Sankyo Company, Limited Amino alcohol compound
TW200505416A (en) * 2003-08-12 2005-02-16 Mitsubishi Pharma Corp Bi-aryl compound having immunosuppressive activity
GB0320638D0 (en) 2003-09-03 2003-10-01 Novartis Ag Organic compounds
GB0329498D0 (en) 2003-12-19 2004-01-28 Novartis Ag Organic compounds
DE102004004719A1 (en) * 2004-01-29 2005-08-18 Basf Ag Process for the preparation of enantiomerically pure aminoalcohols
TWI355934B (en) 2004-02-24 2012-01-11 Sankyo Co Pharmaceutical composition for treatment or prophy
US7521473B2 (en) 2004-02-25 2009-04-21 Wyeth Inhibitors of protein tyrosine phosphatase 1B
US20090163523A1 (en) * 2004-05-03 2009-06-25 Philip Lake Combinations comprising a s1p receptor agonist and a jak3 kinase inhibitor
EP1750722A4 (en) 2004-05-06 2010-03-10 Univ Virginia Novel lysophosphatidic acid receptor selective antagonists
CA2571710A1 (en) 2004-06-24 2006-11-02 Nicholas Valiante Small molecule immunopotentiators and assays for their detection
BRPI0513110A (en) * 2004-07-16 2008-04-29 Kyorin Seiyaku Kk medicament comprising diaryl sulfide compound or diaryl ether compound having a 2-amine-1,3-propanediol structure having a peripherally circulating lymphocyte reducing activity, in combination with an immunosuppressive agent and / or an antiinflammatory agent and expression method for the prevention of side effect
TW200611687A (en) * 2004-07-29 2006-04-16 Sankyo Co Pharmaceutical compositions used for immunosuppressant
CA2574664C (en) 2004-07-30 2013-01-15 Novartis Ag Compound formulations of 2-amino-1,3-propanediol compounds
US7119211B2 (en) * 2004-09-23 2006-10-10 Yamakawa Chemical Industry Co., Ltd. Process for preparing optically active 3-(methylamino)-1-(2-thienyl) propan-1-ol and intermediates for preparation
PL1806338T3 (en) * 2004-10-12 2016-07-29 Kyorin Seiyaku Kk Process for producing 2-amino-2-[2-[4-(3-benzyloxy­phenylthio)-2-chlorophenyl[ethyl]-1,3-propanediol hydrochloride and hydrates thereof. and intermediates the production thereof
WO2006058316A1 (en) 2004-11-29 2006-06-01 Novartis Ag Dosage regimen of an s1p receptor agonist
GB0504544D0 (en) 2005-03-04 2005-04-13 Novartis Ag Organic compounds
GB0519274D0 (en) 2005-09-21 2005-11-02 Arakis Ltd The treatment of neurodegenerative diseases
BRPI0617077A2 (en) * 2005-10-07 2015-01-06 Kyorin Seiyaku Kk THERAPEUTIC AGENT FOR TREATMENT OF LIVER DISEASES CONTAINING 2-AMINE-1, 3-PROPANEDIOL DERIVATIVE AS ACTIVE INGREDIENT, AND METHOD FOR TREATMENT OF LIVER DISEASES
TWI389683B (en) * 2006-02-06 2013-03-21 Kyorin Seiyaku Kk A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient
BRPI0710878A2 (en) 2006-04-11 2015-03-31 Novartis Ag Organic compounds and their uses
GB0612721D0 (en) 2006-06-27 2006-08-09 Novartis Ag Organic compounds
TW200815600A (en) 2006-08-04 2008-04-01 Daiichi Sankyo Co Ltd An enzyme for phosphorizing a medicine
PL2058317T3 (en) * 2006-08-08 2014-03-31 Kyorin Seiyaku Kk Aminophosphoric acid ester derivative and s1p receptor modulator containing the same as active ingredient
US8273748B2 (en) 2006-08-08 2012-09-25 Kyorin Pharmaceutical Co., Ltd. Amino alcohol derivative and immunosuppresive agent having same as an active ingredient
US20100040678A1 (en) 2006-09-26 2010-02-18 Michael Ambuhl Organic compounds
TW200906389A (en) * 2007-05-25 2009-02-16 Daiichi Sankyo Co Ltd Pharmaceutical composition comprising of therapeutic or prophylactic agents for hepatitis
ES2864671T3 (en) 2007-10-12 2021-10-14 Novartis Ag Compositions comprising sphingosine 1-phosphate (s1p) receptor modulators
US8476305B2 (en) 2008-02-07 2013-07-02 Kyorin Pharmaceutical Co., Ltd. Therapeutic agent or prophylactic agent for inflammatory bowel disease comprising amino alcohol derivative as active ingredient
WO2009142194A1 (en) * 2008-05-19 2009-11-26 杏林製薬株式会社 Method for producing optically active aminoalcohol derivative
US20110182850A1 (en) 2009-04-10 2011-07-28 Trixi Brandl Organic compounds and their uses
US8512690B2 (en) 2009-04-10 2013-08-20 Novartis Ag Derivatised proline containing peptide compounds as protease inhibitors
US9011833B2 (en) 2010-10-08 2015-04-21 Novartis Ag Vitamin E formulations of sulfamide NS3 inhibitors
JP2015505536A (en) 2012-01-20 2015-02-23 アクセラ インク． Substituted heterocyclic compounds for the treatment of diseases
WO2018166855A1 (en) 2017-03-16 2018-09-20 Basf Se Heterobicyclic substituted dihydroisoxazoles

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2817494A1 (en) * 1977-05-03 1978-11-09 Continental Pharma AMINO ALCOHOL DERIVATIVE
US4638070A (en) * 1978-12-21 1987-01-20 Continental Pharma Heterocyclic amino-alcohol derivatives
JPS55124742A (en) * 1979-03-20 1980-09-26 Kyowa Hakko Kogyo Co Ltd Novel aminoalcohol derivative
JPS60132934A (en) * 1983-11-21 1985-07-16 Nippon Shinyaku Co Ltd Butanol derivative
GB8405112D0 (en) * 1984-02-28 1984-04-04 Akzo Nv Anti-arrhythmic amino-alcohols
US5250546A (en) * 1984-09-28 1993-10-05 Nippon Chemiphar Co., Ltd. Amino-alcohol derivatives and processes for their preparation
FR2585708B1 (en) * 1985-07-31 1989-07-07 Sanofi Sa RESIN AND ACID PROTEIN INHIBITOR AMINOALCOHOL DERIVATIVES, PREPARATION METHOD THEREOF AND THERAPEUTIC APPLICATION THEREOF
IL86740A (en) * 1987-06-30 1992-11-15 Tanabe Seiyaku Co Thiphene derivatives,their preparation and pharmaceutical compositions containing them
JPH02256612A (en) * 1988-12-22 1990-10-17 Tanabe Seiyaku Co Ltd Regulator for digestive tract function
JP2747849B2 (en) * 1990-08-24 1998-05-06 大鵬薬品工業株式会社 Method for selective acylation of 2'-deoxynucleosides
CA2058185A1 (en) * 1990-12-24 1992-06-25 Manfred Schudok Process for the acylation of alcohols with immobilized enzymes
NO179246C (en) * 1991-11-20 1996-09-04 Sankyo Co Aromatic amino-alcohol derivatives and intermediates for their preparation
WO1993015405A1 (en) * 1992-01-29 1993-08-05 Sci-Clone, Inc. Carcinoma associated antigen (sk1) monoclonal antibodies against sk1, methods of producing these antibodies and use therfor
US5604229A (en) 1992-10-21 1997-02-18 Yoshitomi Pharmaceutical Industries, Ltd. 2-amino-1,3-propanediol compound and immunosuppressant
JP3655629B2 (en) * 1993-06-29 2005-06-02 株式会社カネカ Optically active amino alcohol derivative and process for producing the same
KR100358922B1 (en) 1994-08-22 2003-01-24 미쯔비시 웰 파마 가부시키가이샤 Benzene compound and medicinal use thereof
US5948820A (en) * 1994-08-22 1999-09-07 Yoshitomi Pharmaceutical Industries, Ltd. Benzene compound and pharmaceutical use thereof
JP3794702B2 (en) * 1994-10-12 2006-07-12 バンダービルト・ユニバーシテイ Enzymatic preparation of chiral-α-tertiary carboxylic esters
JPH09124564A (en) * 1995-11-06 1997-05-13 Nikko Rika Kk Optically active compound mixture and its production
NO965193L (en) * 1995-12-08 1997-06-09 Seikagaku Kogyo Kk Seikagaku C Aminal alcohol derivative and process for its preparation
EP0904348B1 (en) * 1996-05-30 2004-11-24 Lonza AG Process for the preparation of amino alcohols and derivatives thereof
WO1998045249A1 (en) 1997-04-04 1998-10-15 Yoshitomi Pharmaceutical Industries, Ltd. 2-aminopropane-1,3-diol compounds, medicinal use thereof, and intermediates in synthesizing the same
US6214823B1 (en) * 1997-10-17 2001-04-10 Merck & Co., Inc. Benzodiazepine derivatives as antiarrhythmic agents
CZ200350A3 (en) * 2000-07-13 2003-05-14 Sankyo Company Limited Aminoalcohol derivatives
JP2004507552A (en) * 2000-08-31 2004-03-11 メルク　エンド　カムパニー　インコーポレーテッド Phosphate derivatives as immunomodulators
US20040058894A1 (en) * 2002-01-18 2004-03-25 Doherty George A. Selective S1P1/Edg1 receptor agonists

Also Published As

Publication number Publication date
NZ523554A (en) 2004-12-24
PL359411A1 (en) 2004-08-23
CN1267429C (en) 2006-08-02
US6964976B2 (en) 2005-11-15
EP1300405A4 (en) 2004-04-21
CN1494540A (en) 2004-05-05
IL174664A0 (en) 2006-08-20
TWI301833B (en) 2008-10-11
EP1300405B1 (en) 2007-04-18
MXPA03000397A (en) 2003-05-27
HUP0301688A3 (en) 2006-05-29
EP1300405A1 (en) 2003-04-09
AU6950301A (en) 2002-01-30
CZ200350A3 (en) 2003-05-14
KR20030047988A (en) 2003-06-18
HUP0301688A2 (en) 2003-09-29
AU2001269503B2 (en) 2005-02-17
WO2002006268A1 (en) 2002-01-24
CN1680563A (en) 2005-10-12
US6723745B2 (en) 2004-04-20
IL153594A (en) 2008-04-13
SK152003A3 (en) 2004-07-07
US20040132784A1 (en) 2004-07-08
CN1328387C (en) 2007-07-25
ATE360011T1 (en) 2007-05-15
NO20030120D0 (en) 2003-01-10
CA2415678A1 (en) 2003-01-10
HK1051680A1 (en) 2003-08-15
US20030236297A1 (en) 2003-12-25
NZ533997A (en) 2005-11-25
KR100812578B1 (en) 2008-03-13
BR0112484A (en) 2003-09-23
DE60127961D1 (en) 2007-05-31
NO20030120L (en) 2003-03-11

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